Suppr超能文献

唐氏综合征中的短暂性骨髓增殖性疾病和急性非淋巴细胞白血病。

Transient myeloproliferative disorder and acute nonlymphoblastic leukemia in Down syndrome.

作者信息

Wong K Y, Jones M M, Srivastava A K, Gruppo R A

机构信息

Division of Hematology-Oncology, Children's Hospital Medical Center, Cincinnati, OH 45229.

出版信息

J Pediatr. 1988 Jan;112(1):18-22. doi: 10.1016/s0022-3476(88)80112-4.

Abstract

Two infants with Down syndrome had transient myeloproliferative disorder (TMD) during the neonatal period and subsequently acute nonlymphoblastic leukemia (ANLL). Histochemically, the blast cells in TMD were indistinguishable from those in ANLL. Only the constitutional chromosome (trisomy 21) was found in TMD, whereas new cytogenetic abnormalities emerged in ANLL. A mixed growth pattern in stem cell cultures during TMD suggested the existence of an abnormal clone that might be responsible for the evolution into ANLL at a later date. Serial cytogenetic studies and culture studies of peripheral blood cells may help to understand the pathophysiology and risk of ANLL in patients with TMD.

摘要

两名唐氏综合征婴儿在新生儿期患有短暂性骨髓增殖性疾病(TMD),随后发展为急性非淋巴细胞白血病(ANLL)。组织化学检查显示,TMD中的原始细胞与ANLL中的无法区分。TMD中仅发现了先天性染色体(21三体),而ANLL中出现了新的细胞遗传学异常。TMD期间干细胞培养的混合生长模式提示存在异常克隆,可能是导致日后发展为ANLL的原因。对外周血细胞进行连续的细胞遗传学研究和培养研究,可能有助于了解TMD患者ANLL的病理生理学和风险。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验